Buschiazzo Jorgelina, Ríos Glenda L, Canizo Jesica R, Antollini Silvia S, Alberio Ricardo H
Biotecnología de la Reproducción, Departamento de Producción Animal, Instituto Nacional de Tecnología Agropecuaria (INTA), EEA Balcarce, Balcarce, Argentina.
Instituto de Investigaciones Bioquímicas de Bahía Blanca (CONICET-UNS), Camino La Carringanda, Bahía Blanca, Argentina.
PLoS One. 2017 Jul 7;12(7):e0180451. doi: 10.1371/journal.pone.0180451. eCollection 2017.
Part of the damage caused by cryopreservation of mammalian oocytes occurs at the plasma membrane. The addition of cholesterol to cell membranes as a strategy to make it more tolerant to cryopreservation has been little addressed in oocytes. In order to increase the survival of bovine oocytes after cryopreservation, we proposed not only to increase cholesterol level of oocyte membranes before vitrification but also to remove the added cholesterol after warming, thus recovering its original level. Results from our study showed that modulation of membrane cholesterol by methyl-β-cyclodextrin (MβCD) did not affect the apoptotic status of oocytes and improved viability after vitrification yielding levels of apoptosis closer to those of fresh oocytes. Fluorometric measurements based on an enzyme-coupled reaction that detects both free cholesterol (membrane) and cholesteryl esters (stored in lipid droplets), revealed that oocytes and cumulus cells present different levels of cholesterol depending on the seasonal period. Variations at membrane cholesterol level of oocytes were enough to account for the differences found in total cholesterol. Differences found in total cholesterol of cumulus cells were explained by the differences found in both the content of membrane cholesterol and of cholesterol esters. Cholesterol was incorporated into the oocyte plasma membrane as evidenced by comparative labeling of a fluorescent cholesterol. Oocytes and cumulus cells increased membrane cholesterol after incubation with MβCD/cholesterol and recovered their original level after cholesterol removal, regardless of the season. Finally, we evaluated the effect of vitrification on the putative raft molecule GM1. Cholesterol modulation also preserved membrane organization by maintaining ganglioside level at the plasma membrane. Results suggest a distinctive cholesterol metabolic status of cumulus-oocyte complexes (COCs) among seasons and a dynamic organizational structure of cholesterol homeostasis within the COC. Modulation of membrane cholesterol by MβCD improved survival of bovine oocytes and preserved integrity of GM1-related rafts after vitrification.
哺乳动物卵母细胞冷冻保存所造成的部分损伤发生在质膜。作为一种使细胞膜更耐受冷冻保存的策略,向细胞膜中添加胆固醇在卵母细胞方面鲜有涉及。为了提高牛卵母细胞冷冻保存后的存活率,我们提出不仅要在玻璃化之前提高卵母细胞膜的胆固醇水平,还要在复温后去除添加的胆固醇,从而恢复其原始水平。我们的研究结果表明,用甲基-β-环糊精(MβCD)调节膜胆固醇不会影响卵母细胞的凋亡状态,并且能提高玻璃化后的活力,使凋亡水平更接近新鲜卵母细胞。基于检测游离胆固醇(膜中)和胆固醇酯(储存于脂滴中)的酶联反应的荧光测量显示,卵母细胞和卵丘细胞的胆固醇水平因季节不同而有所差异。卵母细胞质膜胆固醇水平的变化足以解释总胆固醇的差异。卵丘细胞总胆固醇的差异可由膜胆固醇含量和胆固醇酯含量的差异来解释。荧光胆固醇的比较标记证明胆固醇被整合到卵母细胞质膜中。无论季节如何,卵母细胞和卵丘细胞在与MβCD/胆固醇孵育后膜胆固醇增加,去除胆固醇后恢复到原始水平。最后,我们评估了玻璃化对假定的筏分子GM1的影响。胆固醇调节还通过维持质膜上神经节苷脂水平来保持膜的组织性。结果表明,卵丘-卵母细胞复合体(COC)在不同季节具有独特的胆固醇代谢状态,且COC内胆固醇稳态具有动态组织结构。MβCD调节膜胆固醇可提高牛卵母细胞的存活率,并在玻璃化后保持GM1相关筏的完整性。